Organic Acids
Medchemexpress LLC Ganirelix acetate | 129311-55-3 | 99.19% | 1690.42 | 1 ML
Ganirelix acetate is an injectable competitive gonadotropin-releasing hormone (GnRH) antagonist. It directly competes against the endogenous molecule for receptor binding, leading to a rapid reduction in estradiol levels. It can be used for researching ovarian hyperstimulation syndrome (OHSS).
- Targets GnRH with an IC50 of 3.6 nM in HEK293 cells
- Antagonizes human GnHR receptor activity
- Suitable for research on ovarian hyperstimulation syndrome (OHSS)
- Causes rapid reduction in estradiol levels
Rowley Biochemical Institute Inc GLACIAL ACETIC ACID
Glacial Acetic Acid - 1 Quart - Part Number SO-618-QT - Also Available in 8oz Pint and Gallon from Rowley BioChemical
Alkali Scientific Acetic Acid, Glacial, 500 Milliliters
Acetic Acid, Glacial, 500mL is a concentrated laboratory reagent used primarily in chemical synthesis, pH adjustment, and buffer preparation. The glacial form of acetic acid is highly acidic, making it an ideal reagent for use in analytical chemistry and biological assays that require a low pH environment. It is also frequently used as a solvent and acidifying agent in various reactions, including esterification and acylation. The 500mL size is well-suited for small-scale laboratory procedures, offering precision and convenience while maintaining the purity and potency of glacial acetic acid in controlled experimental settings.
Research Products International Corp Acetic Acid, Glacial, 4 Liters
Acetic acid (CH₃COOH) is a colorless, corrosive liquid with a strong odor, fully miscible in water. With a molecular weight of 60.05 g/mol, it is used in life science labs for buffer preparation, protein precipitation, histological staining, pH regulation, and as a solvent in various biochemical and molecular procedures.
Medchemexpress LLC ω-Agatoxin IVA TFA | 99.1% | 5316.27 | 1 MG
ω-Agatoxin IVA TFA is a potent and selective blocker of P/Q-type Ca2+ (Cav2.1) channels. It inhibits glutamate exocytosis and calcium influx induced by high potassium, and blocks the high potassium-induced release of serotonin and norepinephrine. This compound does not affect L-type or N-type calcium channels.
- Potent and selective blocker of P/Q-type Ca2+ (Cav2.1) channels
- Inhibits glutamate exocytosis and calcium influx induced by high potassium
- Blocks high potassium-induced release of serotonin and norepinephrine
- Does not affect L-type or N-type calcium channels
Medchemexpress LLC Pep2-8 TFA | 98.8% | 1715.85 (free base) | 1 MG
Pep2-8 is a peptide that enhances the antagonistic activity of proprotein convertase subtilin/kexin type 9 (PCSK9). It binds to C-terminally truncated PCSK9 and restored LDL uptake of PCSK9-treated HepG2 cells to approximately 90% of control activity at a concentration of 50 μM.
- Enhances antagonistic activity of proprotein convertase subtilin/kexin type 9 (PCSK9)
- Binds to C-terminally truncated PCSK9
- Restores LDL uptake of PCSK9-treated HepG2 cells to approximately 90% of control activity
- For research use only
Medchemexpress LLC SAR441255 (TFA) | 99.9% | 4866.56 | 25 MG
SAR441255 TFA is a potent unimolecular peptide GLP-1/GIP/GCG receptor triagonist. It displays high potency with balanced activation of all three target receptors and shows positive acute glucoregulatory effects in diabetic obese monkeys.
- Potent unimolecular peptide GLP-1/GIP/GCG receptor triagonist.
- Displays high potency with balanced activation of all three target receptors.
- Shows positive acute glucoregulatory effects in diabetic obese monkeys.
Apexbio Technology LLC BIBP 3226 trifluoroacetate(Synonyms: BIBP3226 TFA, BIBP3226 trifluoroacetate salt, NPY Y1 receptor antagonist BIBP3226), 2mg, CAS: 1068148-47-9.
BIBP 3226 trifluoroacetate (CAS 1068148-47-9) is a non-peptide antagonist targeting neuropeptide Y Y1 (NPY Y1) and neuropeptide FF (NPFF) receptors showing binding affinity with Ki values of 1 1 nM (rNPY Y1) 79 nM (hNPFF2) and 108 nM (rNPFF) BIBP 3226 competes with NPFF prevents NPFF-induced inhibition of forskolin-stimulated cAMP production and blocks NPFF-dependent hypothermic and anti-opioid effects in rodent models This compound is employed experimentally to investigate NPY/NPFF system roles in anxiety analgesia and cardiovascular regulation
Medchemexpress LLC Z-VRPR-FMK TFA (VRPR) | 95.0% | 790.81 | 200 UG
Z-VRPR-FMK TFA (VRPR) is a tetrapeptide and a selective, irreversible MALT1 (Mucosa-associated lymphoid tissue lymphoma translocation protein 1) inhibitor. It can protect against influenza A virus (IAV) infection.
- Selective and irreversible MALT1 inhibitor
- Protects against influenza A virus (IAV) infection
Medchemexpress LLC Cys-TAT(47-57) TFA | 98.1% | 1661.99 | 10 MG
Cys-TAT(47-57) (Cys-[HIV-Tat (47-57)]) is an arginine rich cell penetrating peptide derived from the HIV-1 transactivating protein. This product is intended for research use only and is not sold to patients.
- Purity: 98.1%
- Molecular weight: 1661.99 (free base)
- Appearance: Solid
- Color: White to off-white
- Solubility in H2O: 100 mg/mL (ultrasonic needed)
- Solubility in DMSO: ≥ 100 mg/mL
Medchemexpress LLC Citric acid-13C6 | 287389-42-8 | MFCD01075573 | 99.9% | 198.08 | 13C6H8O7 | 10 MG
Isotopically labeled citric acid with all six carbons as 13C, provided as a high-purity stable isotope reagent for use as a tracer or internal standard in analytical methods such as NMR, GC-MS, and LC-MS. Supplied as a 10 mg solid with recommended sealed storage away from moisture.
- High isotopic enrichment suitable for quantitative analysis.
- High purity for accurate analytical results.
- Suitable as tracer or internal standard for NMR, GC-MS, LC-MS.
- Solid form; easy to weigh and dissolve for standards.
- Recommended sealed storage away from moisture to preserve stability.
Medchemexpress LLC Calcitonin, eel TFA | 99.9% | 3528.89 | 5 MG
Calcitonin, eel TFA is a thyroid hormone peptide that plays a role in regulating calcium homeostasis. It is frequently used in research concerning postmenopausal osteoporosis. In vitro studies show that Calcitonin, eel stimulates phosphoinositide hydrolysis and prolactin release in cultured anterior pituitary cells more effectively than salmon calcitonin. However, it does not inhibit prolactin release under conditions stimulated by thyrotropin releasing hormone (TRH).
- Contributes to the regulation of calcium homeostasis.
- Widely used in postmenopausal osteoporosis research.
- Effectively induces a concentration-dependent stimulation of phosphoinositide hydrolysis in vitro.
- Stimulates prolactin release in cultured anterior pituitary cells in vitro.
- High purity of 99.91%.
